Sui Yu

949 total citations
18 papers, 594 citations indexed

About

Sui Yu is a scholar working on Genetics, Molecular Biology and Atomic and Molecular Physics, and Optics. According to data from OpenAlex, Sui Yu has authored 18 papers receiving a total of 594 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 6 papers in Atomic and Molecular Physics, and Optics. Recurrent topics in Sui Yu's work include Genetics and Neurodevelopmental Disorders (7 papers), Advanced Fiber Laser Technologies (6 papers) and Genomics and Rare Diseases (5 papers). Sui Yu is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Advanced Fiber Laser Technologies (6 papers) and Genomics and Rare Diseases (5 papers). Sui Yu collaborates with scholars based in China, Australia and United States. Sui Yu's co-authors include Robert I. Richards, Grant R. Sutherland, D. Hewett, Marie Mangelsdorf, Lynne Hobson, Helen J. Eyre, Norman A. Doggett, Naras M. Lapsys, Elizabeth Baker and Denis Le Paslier and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

Sui Yu

16 papers receiving 558 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Sui Yu China	9	387	307	104	51	37	18	594
Zhuozhi Wang Canada	12	280 0.7×	355 1.2×	128 1.2×	40 0.8×	68 1.8×	21	710
Megan T. Cho United States	20	462 1.2×	508 1.7×	79 0.8×	46 0.9×	65 1.8×	27	838
Naghmeh Dorrani United States	12	367 0.9×	314 1.0×	132 1.3×	11 0.2×	37 1.0×	20	518
Cécile Mignon‐Ravix France	15	320 0.8×	475 1.5×	24 0.2×	62 1.2×	90 2.4×	26	727
Ellen Taub Israel	8	263 0.7×	207 0.7×	121 1.2×	26 0.5×	88 2.4×	12	446
Tiia Reimand Estonia	13	291 0.8×	229 0.7×	21 0.2×	52 1.0×	97 2.6×	41	488
Yoonha Lee South Korea	9	471 1.2×	300 1.0×	373 3.6×	47 0.9×	29 0.8×	23	775
Tetsushi Yamagata Japan	12	276 0.7×	448 1.5×	82 0.8×	221 4.3×	32 0.9×	14	736
Shashidhar Pai United States	8	237 0.6×	278 0.9×	61 0.6×	10 0.2×	49 1.3×	13	391

Countries citing papers authored by Sui Yu

Since Specialization

Citations

This map shows the geographic impact of Sui Yu's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sui Yu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sui Yu more than expected).

Fields of papers citing papers by Sui Yu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sui Yu. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sui Yu. The network helps show where Sui Yu may publish in the future.

Co-authorship network of co-authors of Sui Yu

This figure shows the co-authorship network connecting the top 25 collaborators of Sui Yu. A scholar is included among the top collaborators of Sui Yu based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sui Yu. Sui Yu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

18 of 18 papers shown

Song, Yuhong, Zepeng Liu, Sui Yu, et al.. (2024). Mode-locked switchable fiber laser based on Mamyshev oscillator cavity with anomalous dispersion gain fiber. Chaos Solitons & Fractals. 187. 115386–115386.

Yu, Sui, et al.. (2024). High signal-to-noise ratio harmonic mode-locking Mamyshev oscillator at 1550 nm. Optics Communications. 569. 130787–130787. 2 indexed citations

Kou, Shan Shan, Min Ye, Sui Yu, et al.. (2024). Activation of Imprinted Gene PW1 Promotes Cardiac Fibrosis After Ischemic Injury. Circulation. 151(9). 623–639. 4 indexed citations

Liu, Yikai, Sui Yu, Yuhong Song, et al.. (2023). All-fiber spatiotemporal mode-locked based on Mamyshev mechanism with high energy noise-like pulse generation at 1550 nm. Optics Communications. 552. 130074–130074. 4 indexed citations

Liu, Yikai, et al.. (2023). High repetition frequency spatiotemporal mode-locked fiber laser based on cavity induced modulation instability. Optics & Laser Technology. 171. 110346–110346. 1 indexed citations

Yu, Sui, et al.. (2023). Expression analysis of plvap in mouse heart development, homeostasis and injury. Gene Expression Patterns. 50. 119343–119343. 1 indexed citations

Yu, Sui, Yikai Liu, Chongyang Xu, et al.. (2023). 2.11 GHz all-fiber harmonic mode-locked laser based on highly nonlinear hybrid multimode interference saturable absorber. Optics Communications. 545. 129632–129632. 1 indexed citations

Yu, Sui, et al.. (2023). Harmonic Mode-Locking From Erbium-Doped Fiber Self-Starting Mamyshev Oscillator. Journal of Lightwave Technology. 42(5). 1605–1610. 8 indexed citations

Niemi, Mari, Hilary C. Martin, Daniel L Rice, et al.. (2018). Common genetic variants contribute to risk of rare severe neurodevelopmental disorders. Nature. 562(7726). 268–271. 184 indexed citations

10.

Mordaunt, Dylan, Shanti Balasubramaniam, David R. Thorburn, et al.. (2015). Phenotypic variation of TTC19‐deficient mitochondrial complex III deficiency: A case report and literature review. American Journal of Medical Genetics Part A. 167(6). 1330–1336. 26 indexed citations

11.

Haan, Eric, et al.. (2014). Phenotypes of AKT3 deletion: A case report and literature review. American Journal of Medical Genetics Part A. 167(1). 174–179. 36 indexed citations

12.

Huang, Yue, Sui Yu, Zhanhe Wu, & Beisha Tang. (2014). Genetics of hereditary neurological disorders in children.. PubMed. 3(2). 108–19. 14 indexed citations

13.

Nicholl, Jillian, Susan J. Brown, Michael Harbord, et al.. (2012). Epilepsy with cognitive deficit and autism spectrum disorders: Prospective diagnosis by array CGH. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(1). 24–35. 17 indexed citations

14.

Xu, Wei, Miao Jiang, Ning Zhao, et al.. (2010). Detecting the TGFA gene Taq I mutation with high resolution melting method.. 39(4). 281–285. 1 indexed citations

15.

McMahon, Jacinta M., Ingrid E. Scheffer, Jillian Nicholl, et al.. (2010). Detection of microchromosomal aberrations in refractory epilepsy: a pilot study. Epileptic Disorders. 12(3). 192–198. 14 indexed citations

16.

Yu, Sui, Marie Mangelsdorf, D. Hewett, et al.. (1997). Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat. Cell. 88(3). 367–374. 155 indexed citations

17.

Horwitz, Marshall S., Kathleen F. Benson, John Wolff, et al.. (1997). Genetic Heterogeneity in Familial Acute Myelogenous Leukemia: Evidence for a Second Locus at Chromosome 16q21-23.2. The American Journal of Human Genetics. 61(4). 873–881. 32 indexed citations

18.

Sutherland, Grant R., Ági K. Gedeon, Louise Kornman, et al.. (1991). Prenatal Diagnosis of Fragile X Syndrome by Direct Detection of the Unstable DNA Sequence. New England Journal of Medicine. 325(24). 1720–1722. 94 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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